Canonical Allele Identifier: PA2828360956
Gene: SCN8A HGNC NCBI

Linked Data

ClinVar Variation Id: 436670

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356717.1:p.Arg1055Gln
CA6571555
NM_001369788.1:c.3164G>A